Hereditary recurrent focal neuropathies: clinical and molecular features.
about
The PMP22 gene and its related diseases.Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease.Inherited peripheral neuropathies.PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies.Neuromuscular ultrasound in polyneuropathies and motor neuron disease.Sphingosine 1-phosphate lyase deficiency causes Charcot-Marie-Tooth neuropathy.Hereditary neuropathy with liability to pressure palsies: case report and discussion.Rapidly progressive amyotrophic lateral sclerosis in a young patient with hereditary neuropathy with liability to pressure palsies.Hereditary neuropathy with liability to pressure palsies and anaesthesia: peri-operative nerve injury.
P2860
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P2860
Hereditary recurrent focal neuropathies: clinical and molecular features.
description
2000 nî lūn-bûn
@nan
2000 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2000年の論文
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2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Hereditary recurrent focal neuropathies: clinical and molecular features.
@ast
Hereditary recurrent focal neuropathies: clinical and molecular features.
@en
type
label
Hereditary recurrent focal neuropathies: clinical and molecular features.
@ast
Hereditary recurrent focal neuropathies: clinical and molecular features.
@en
prefLabel
Hereditary recurrent focal neuropathies: clinical and molecular features.
@ast
Hereditary recurrent focal neuropathies: clinical and molecular features.
@en
P2093
P356
P1433
P1476
Hereditary recurrent focal neuropathies: clinical and molecular features.
@en
P2093
De Jonghe P
Kuhlenbäumer G
Stögbauer F
Timmerman V
P304
P356
10.1212/WNL.54.3.546
P407
P577
2000-02-01T00:00:00Z